NL-OMON51678招募中不适用
Repetitive Transcranial Magnetic Stimulation (rTMS) versus sham rTMS in Body Dysmorphic Disorder - rTMS-BDD
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 56
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 64(—)
入选标准
- •1. Age 18 to 65 years old;
- •2. Diagnosed with Body Dysmorphic Disorder (BDD), based on Body Dysmorphic
- •Disorder - Yale Brown Obsessive Compulsive Scale (BDD-YBOCS);
- •3. Nonresponse (defined as <50% response on symptoms measured by the BDD-YBOCS)
- •after one type of medication treatment, SSRI, maximum dose and adequate
- •4. Medication is set 6 weeks prior to the start, and could not be changed
- •during the study
排除标准
- •Exclusion criteria
- •1. Intracerebral metal implants (e.g. cochlear implant, brain stimulator);
- •2. (History of) epilepsy or epilepsy in a first degree relative;
- •3. Any other neurological disorder with seizure risk;
- •4. Acute suicidal ideations, or any psychological crisis (contact with the
- •outpatient crisis service or admission in psychiatric hospital);
- •5. Bipolar disorder;
- •6. Current disorder in substance abuse (opiate, ketamine, LSD,
- •(meth)amphetamine, cocaine, solvents, cannabis, benzodiazepines or barbiturate)
- •or alcohol abuse;
- •7. Any known other serious somatic health problem;
- •8. Pregnancy;
- •9. Primarily autism spectrum disorder or primarily personality disorder (using
- •SCID-5-P at baseline for personality disorders). Given that this is often seen
- •secondarily in BDD patients.
- •rTMS Contraindications:
- •1. History of epileptic seizures or epilepsy in a first degree relative,
- •irregular sleep/ wake rhythm;
- •2. Cardiac demand pacemakers;
- •3. Implanted defibrillators;
- •4. Implanted neurostimulators;
- •5. Cochlear implants.
研究者
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